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A purine salvage bottleneck leads to bacterial adenine cross-feeding

Diverse ecosystems host microbial relationships that are stabilized by nutrient cross-feeding. Cross-feeding can involve metabolites that should hold value for the producer. Externalization of such communally valuable metabolites is often unexpected and difficult to predict. Previously, we fortuitou...

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Autores principales: Chuang, Ying-Chih, Haas, Nicholas W., Pepin, Robert, Behringer, Megan, Oda, Yasuhiro, LaSarre, Breah, Harwood, Caroline S., McKinlay, James B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10614841/
https://www.ncbi.nlm.nih.gov/pubmed/37904951
http://dx.doi.org/10.1101/2023.10.17.562681
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author Chuang, Ying-Chih
Haas, Nicholas W.
Pepin, Robert
Behringer, Megan
Oda, Yasuhiro
LaSarre, Breah
Harwood, Caroline S.
McKinlay, James B.
author_facet Chuang, Ying-Chih
Haas, Nicholas W.
Pepin, Robert
Behringer, Megan
Oda, Yasuhiro
LaSarre, Breah
Harwood, Caroline S.
McKinlay, James B.
author_sort Chuang, Ying-Chih
collection PubMed
description Diverse ecosystems host microbial relationships that are stabilized by nutrient cross-feeding. Cross-feeding can involve metabolites that should hold value for the producer. Externalization of such communally valuable metabolites is often unexpected and difficult to predict. Previously, we fortuitously discovered purine externalization by Rhodopseudomonas palustris by its ability to rescue growth of an Escherichia coli purine auxotroph. Here we found that an E. coli purine auxotroph can stably coexist with R. palustris due to purine cross-feeding. We identified the cross-fed purine as adenine. Adenine was externalized by R. palustris under diverse growth conditions. Computational models suggested that adenine externalization occurs via passive diffusion across the cytoplasmic membrane. RNAseq analysis led us to hypothesize that accumulation and externalization of adenine stems from an adenine salvage bottleneck at the enzyme encoded by apt. Ectopic expression of apt eliminated adenine externalization, supporting our hypothesis. A comparison of 49 R. palustris strains suggested that purine externalization is relatively common, with 15 of the strains exhibiting the trait. Purine externalization was correlated with the genomic orientation of apt orientation, but apt orientation alone could not explain adenine externalization in some strains. Our results provide a mechanistic understanding of how a communally valuable metabolite can participate in cross-feeding. Our findings also highlight the challenge in identifying genetic signatures for metabolite externalization.
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spelling pubmed-106148412023-10-31 A purine salvage bottleneck leads to bacterial adenine cross-feeding Chuang, Ying-Chih Haas, Nicholas W. Pepin, Robert Behringer, Megan Oda, Yasuhiro LaSarre, Breah Harwood, Caroline S. McKinlay, James B. bioRxiv Article Diverse ecosystems host microbial relationships that are stabilized by nutrient cross-feeding. Cross-feeding can involve metabolites that should hold value for the producer. Externalization of such communally valuable metabolites is often unexpected and difficult to predict. Previously, we fortuitously discovered purine externalization by Rhodopseudomonas palustris by its ability to rescue growth of an Escherichia coli purine auxotroph. Here we found that an E. coli purine auxotroph can stably coexist with R. palustris due to purine cross-feeding. We identified the cross-fed purine as adenine. Adenine was externalized by R. palustris under diverse growth conditions. Computational models suggested that adenine externalization occurs via passive diffusion across the cytoplasmic membrane. RNAseq analysis led us to hypothesize that accumulation and externalization of adenine stems from an adenine salvage bottleneck at the enzyme encoded by apt. Ectopic expression of apt eliminated adenine externalization, supporting our hypothesis. A comparison of 49 R. palustris strains suggested that purine externalization is relatively common, with 15 of the strains exhibiting the trait. Purine externalization was correlated with the genomic orientation of apt orientation, but apt orientation alone could not explain adenine externalization in some strains. Our results provide a mechanistic understanding of how a communally valuable metabolite can participate in cross-feeding. Our findings also highlight the challenge in identifying genetic signatures for metabolite externalization. Cold Spring Harbor Laboratory 2023-10-17 /pmc/articles/PMC10614841/ /pubmed/37904951 http://dx.doi.org/10.1101/2023.10.17.562681 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Chuang, Ying-Chih
Haas, Nicholas W.
Pepin, Robert
Behringer, Megan
Oda, Yasuhiro
LaSarre, Breah
Harwood, Caroline S.
McKinlay, James B.
A purine salvage bottleneck leads to bacterial adenine cross-feeding
title A purine salvage bottleneck leads to bacterial adenine cross-feeding
title_full A purine salvage bottleneck leads to bacterial adenine cross-feeding
title_fullStr A purine salvage bottleneck leads to bacterial adenine cross-feeding
title_full_unstemmed A purine salvage bottleneck leads to bacterial adenine cross-feeding
title_short A purine salvage bottleneck leads to bacterial adenine cross-feeding
title_sort purine salvage bottleneck leads to bacterial adenine cross-feeding
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10614841/
https://www.ncbi.nlm.nih.gov/pubmed/37904951
http://dx.doi.org/10.1101/2023.10.17.562681
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